The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
122756772 12275677 2 F 20160901 20160418 20160902 EXP CA-ROCHE-1741799 ROCHE 77.00 YR F Y 0.00000 20160902 OT CA CA

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
122756772 12275677 1 PS ESBRIET PIRFENIDONE 1 Unknown U 22535 9 DF CAPSULE QD
122756772 12275677 2 SS ESBRIET PIRFENIDONE 1 Unknown U 22535 CAPSULE
122756772 12275677 3 SS PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 Unknown U 0 200 MG TABLET BID
122756772 12275677 4 SS XELJANZ TOFACITINIB CITRATE 1 Oral U 0 5 MG BID
122756772 12275677 5 SS XELJANZ TOFACITINIB CITRATE 1 Oral FOR 6 MONTHS U 0 5 MG TABLET BID
122756772 12275677 6 C PREDNISONE. PREDNISONE 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122756772 12275677 1 Product used for unknown indication
122756772 12275677 3 Rheumatoid arthritis
122756772 12275677 4 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
122756772 12275677 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
122756772 12275677 Arthralgia
122756772 12275677 Bronchitis
122756772 12275677 Cystitis
122756772 12275677 Diarrhoea
122756772 12275677 Dizziness
122756772 12275677 Nausea
122756772 12275677 Pneumonia
122756772 12275677 Urinary tract infection

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found